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. 2019 Jul 9;5(1):25.
doi: 10.1186/s40729-019-0178-2.

Cytotoxicity and proinflammatory effects of titanium and zirconia particles

Affiliations

Cytotoxicity and proinflammatory effects of titanium and zirconia particles

Frank Schwarz et al. Int J Implant Dent. .

Abstract

Background: To assess the effects of differently sized titanium (Ti) and zirconia (Zr) particles on (1) the metabolic activity of osteosarcoma-derived osteoblasts (SaOs-2) and human gingival fibroblasts (HGF) and (2) the cytokine expression of monocytes (THP-1) METHODS: Ti (60-80 nm and 100 nm) and Zr (2 μm and 75 μm) particles were incubated with SaOs-2, HGF, and THP-1 cells. At days 0, 2, 4, and 7 and 0, 1, 2, and 4 (THP-1), the mitochondrial activity was assessed and enzyme-linked immunosorbent assays were used to determine interleukin (IL)-1 beta and IL-6 concentrations of stimulated THP-1 at day 1.

Results: Ti60-80, Ti100, Zr2, and Zr75 particles were associated with gradual and significant within-group decreases in the viability of SaOs-2 and HGF cells. These effects were less pronounced in the Zr group. Similar to control cells, THP-1 did not reveal any significant increases in IL-1 beta and IL-6 concentrations. Viability of THP-1 was merely impaired in the presence of Ti100.

Conclusions: Ti and Zr particles had a detrimental effect on the viability of SaOs-2 and HGF, but no proinflammatory effect on THP-1.

Keywords: Cellular immunology; Cytokines; Fibroblast; In vitro model; Monocytes; Osteoblast.

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Conflict of interest statement

Frank Schwarz, Maike Langer, Tina Hagena, Brigitte Hartig, Robert Sader, and Jürgen Becker declare that they have no competing interests related to this analysis.

Figures

Fig. 1
Fig. 1
Mitochondrial activity expressed as median luminescent output (counts per second -CPS) of SaOs-2 and HGF in different groups. a Test groups (SaOs-2). b Control group (SaOs-2). c Test groups (HGF). d Control group (HGF). e Test groups (THP-1). f Control groups (THP-1)

References

    1. Berglundh T, Armitage G, Araujo MG, et al. Peri-implant diseases and conditions: consensus report of workgroup 4 of the 2017 world workshop on the classification of periodontal and Peri-implant diseases and conditions. J Clin Periodontol. 2018;45:286–291. doi: 10.1111/jcpe.12957. - DOI - PubMed
    1. Fretwurst T, Nelson K, Tarnow DP, Wang HL, Giannobile WV. Is metal particle release associated with Peri-implant bone destruction? An emerging concept. J Dent Res. 2018;97:259–265. doi: 10.1177/0022034517740560. - DOI - PubMed
    1. Noronha Oliveira M, Schunemann WVH, Mathew MT, et al. Can degradation products released from dental implants affect peri-implant tissues? J Periodontal Res. 2018;53:1–11. doi: 10.1111/jre.12479. - DOI - PubMed
    1. Senna P, Antoninha Del Bel Cury A, Kates S, Meirelles L. Surface damage on dental implants with release of loose particles after insertion into bone. Clin Implant Dent Relat Res. 2015;17:681–692. doi: 10.1111/cid.12167. - DOI - PMC - PubMed
    1. Sikora Craig L., Alfaro Maria F., Yuan Judy Chia-Chun, Barao Valentim A., Sukotjo Cortino, Mathew Mathew T. Wear and Corrosion Interactions at the Titanium/Zirconia Interface: Dental Implant Application. Journal of Prosthodontics. 2018;27(9):842–852. doi: 10.1111/jopr.12769. - DOI - PubMed

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